Determination of Voriconazole in Human Plasma by Liquid Chromatography Tandem Mass Spectrometry: Application in Therapeutic Drug Monitoring

Waleed Alhussaini, Ezzeldeen Ghanem, Magd Alsahly, Amani Kurdi, Eman Alharbi, Imadul Islam, Majed Aljeraisy
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Abstract

A sensitive, accurate and robust Liquid Chromatography Tandem Mass Spectrometry method has been developed and validated to measure voriconazole trough levels in human plasma. The plasma samples were mixed with fluconazole as an Internal Standard and directed to protein precipitation and drug extraction. An aliquot of 1 μl was injected into the chromatographic system and separated by the Acquity BEH C18 column at a flow rate of 0.30 ml/min in a gradient mobile phase consisting of acetonitrile, Ultrapure water (UPW), methanol and formic acid. Voriconazole was detected by a Triple Quadrupole Detector (TQD) operating on Multiple Reaction Monitoring (MRM) and a positive ion mode Electrospray ionization (ESI) Q1 mass: 350.1 m/z, Q3 mass: 281.1 m/z. Method linearity of the calibration curve (0.10 - 8.00 μg/ml) indicated a correlation coefficient r ≥ 0.99. The intra and inter-assay accuracy was within 85% - 115% and the intra and inter-assay precision was ≤5.76%. Voriconazole recovery percentage was between 97.69 - 119.62%. The method was successively applied in routine voriconazole TDM.
液相色谱串联质谱法测定人血浆中伏立康唑:在治疗药物监测中的应用
建立并验证了一种灵敏、准确、可靠的液相色谱串联质谱法测定人血浆中伏立康唑谷浓度的方法。血浆样品与氟康唑混合作为内标,用于蛋白质沉淀和药物提取。在乙腈、超纯水(UPW)、甲醇、甲酸组成的梯度流动相中,以0.30 ml/min的流速,将1 μl的等温物注入色谱系统,用Acquity BEH C18色谱柱分离。伏立康唑的检测采用多反应监测(MRM)三重四极杆检测器(TQD)和正离子模式电喷雾电离(ESI), Q1质量:350.1 m/z, Q3质量:281.1 m/z。方法在0.10 ~ 8.00 μg/ml范围内线性关系良好,相关系数r≥0.99。检测准确度在85% ~ 115%之间,检测准确度≤5.76%。伏立康唑回收率在97.69 ~ 119.62%之间。方法应用于常规伏立康唑TDM。
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